Llamosas-Falcón Laura, Probst Charlotte, Buckley Charlotte, Jiang Huan, Lasserre Aurélie M, Puka Klajdi, Tran Alexander, Rehm Jürgen
Institute for Mental Health Policy Research, Centre for Addiction and Mental Health, Toronto, ON, Canada.
Heidelberg Institute of Global Health, Medical Faculty and University Hospital, Heidelberg, Germany.
Front Gastroenterol (Lausanne). 2022;1. doi: 10.3389/fgstr.2022.1005729. Epub 2022 Oct 13.
Different studies have shown that females develop liver diseases at lower levels of alcohol consumption than males. Our aim was to quantify the dose-response relationship between alcohol consumption and the risk of liver cirrhosis by sex and identify the differences between females and males. A systematic review was conducted using PubMed/Medline and Embase to identify longitudinal and case-control studies that analyzed the relationship between the level of alcohol use and liver cirrhosis (LC) incidence, and mortality (ICD-8 and ICD-9 codes 571 and ICD-10 codes K70, K73, K74). Pooled relative risks (RR) were calculated by random effects models. Restricted cubic splines were used to model the dose-response relationship. A total of 24 studies were included in the analysis. There were collectively 2,112,476 females and 924,853 males, and a total of 4,301 and 4,231 cases of LC for females and males, respectively. We identified a non-linear dose-response relationship. Females showed a higher risk for LC compared to males with the same amount of alcohol consumed daily. For instance, drinking 40 g/day showed RRs of 9.35 (95% CI 7.64-11.45) in females and 2.82 (95% CI 2.53-3.14) in males, while drinking 80 g/day presented RRs of 23.32 (95% CI 18.24-29.82) in females and 7.93 (95% CI 7.12-8.83) in males. Additional analyses showed that a higher risk for females was found for morbidity and for mortality. Understanding the influence of sex on the association of alcohol consumption and the risk of LC is needed to develop recommendations and clinical guidelines for prevention and treatment.
https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022299680, identifier CRD42022299680.
不同研究表明,女性在饮酒量低于男性的情况下就会患上肝脏疾病。我们的目的是量化按性别划分的酒精摄入量与肝硬化风险之间的剂量反应关系,并确定女性和男性之间的差异。使用PubMed/Medline和Embase进行了一项系统综述,以确定分析饮酒水平与肝硬化(LC)发病率及死亡率(ICD - 8和ICD - 9编码571以及ICD - 10编码K70、K73、K74)之间关系的纵向研究和病例对照研究。通过随机效应模型计算合并相对风险(RR)。使用受限立方样条来模拟剂量反应关系。分析共纳入24项研究。女性共有2,112,476人,男性共有924,853人,女性和男性的LC病例分别有4,301例和4,231例。我们确定了一种非线性剂量反应关系。与每日饮酒量相同的男性相比,女性患LC的风险更高。例如,每天饮用40克酒精时,女性的RR为9.35(95%置信区间7.64 - 11.45),男性为2.82(95%置信区间2.53 - 3.14);而每天饮用80克酒精时,女性的RR为23.32(95%置信区间18.24 - 29.82),男性为7.93(95%置信区间7.12 - 8.83)。进一步分析表明,女性在发病率和死亡率方面风险更高。为制定预防和治疗的建议及临床指南,需要了解性别对酒精消费与LC风险关联的影响。
https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022299680,标识符CRD42022299680。